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The SI unit of molar absorption coefficient is the square metre per mole (m 2 /mol), but in practice, quantities are usually expressed in terms of M −1 ⋅cm −1 or L⋅mol −1 ⋅cm −1 (the latter two units are both equal to 0.1 m 2 /mol).
A. R. Forouhi and I. Bloomer deduced dispersion equations for the refractive index, n, and extinction coefficient, k, which were published in 1986 [1] and 1988. [2] The 1986 publication relates to amorphous materials, while the 1988 publication relates to crystalline.
Extinction coefficient refers to several different measures of the absorption of light in a medium: Attenuation coefficient , sometimes called "extinction coefficient" in meteorology or climatology Mass extinction coefficient , how strongly a substance absorbs light at a given wavelength, per mass density
An electromagnetic wave propagating in the +z-direction is conventionally described by the equation: (,) = [()], where E 0 is a vector in the x-y plane, with the units of an electric field (the vector is in general a complex vector, to allow for all possible polarizations and phases);
Therefore, measurements at two wavelengths yields two equations in two unknowns and will suffice to determine the amount concentrations c 1 and c 2 as long as the molar attenuation coefficients of the two components, ε 1 and ε 2 are known at both wavelengths. This two system equation can be solved using Cramer's rule.
(*) The molar extinction is calculated by the number of tyrosines (Y), and the number of disulfide bonding pairs (cystines). Then the following formula is used to calculate the first extinction coefficient: W*5500 + Y*1490 + cystines*125. This calculation assumes that all cysteines pair into cystines.
These two different types of hemoglobin exhibit different absorption spectra that are normally represented in terms of molar extinction coefficients, as shown in Figure 1. The molar extinction coefficient of Hb has its highest absorption peak at 420 nm and a second peak at 580 nm. Its spectrum then gradually decreases as light wavelength increases.
Variable pathlength absorption spectroscopy uses a determined slope to calculate concentration. As stated above this is a product of the molar absorptivity and the concentration. Since the actual absorbance value is taken at many data points at equal intervals, background subtraction is generally unnecessary.